Lenus Infusionstechnik GmbH & Co.KG
DE-MF-000021230 · Germany · Kiel
Lenus Infusionstechnik GmbH & Co.KG is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|
Most frequent device types declared: TPN Spike.
Among these devices, 9 are declared sterile.
Devices declared under this manufacturer
- LENUS Infusion Set Neuraxial PCA - Bag 150ml
- LENUS Infusion Set Neuraxial PCA - Bag 300ml
- LENUS Infusion Set Neuraxial PCA - Bag 50ml
- LENUS Infusion Set Neuraxial PCA - Spike
- LENUS Infusion Set Standard PCA - 150ml
- LENUS Infusion Set Standard PCA - 300ml
- LENUS Infusion Set Standard PCA - Bag 50ml
- LENUS Infusion Set Standard PCA - Spike
- LENUS Infusion Set Standard TPN - Spike
Catalogue references include 123-603, 123-605, 123-606, 123-607, 123-608, 123-615.
European nomenclature codes declared: Z12030385.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 9 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. Lenus Infusionstechnik GmbH & Co.KG was not found in either the U.S. or the Canadian register.